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4-(2-Hydroxyethyl)-8a-methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on | 130594-78-4

中文名称
——
中文别名
——
英文名称
4-(2-Hydroxyethyl)-8a-methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on
英文别名
4-(2-Hydroxyethyl)-8a-methoxy-2,3-dihydro-1,4-benzoxazin-6-one
4-(2-Hydroxyethyl)-8a-methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on化学式
CAS
130594-78-4
化学式
C11H15NO4
mdl
——
分子量
225.244
InChiKey
DIXUSHHOLRMFDE-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -0.8
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.55
  • 拓扑面积:
    59
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    重氮乙烷4-(2-Hydroxyethyl)-8a-methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on甲醇乙醚 为溶剂, 反应 12.0h, 以90%的产率得到(6aR,9R,9aS,9bS)-4-(2-hydroxyethyl)-9b-methoxy-9-methyl-3,6a,9,9a-tetrahydro-2H-pyrazolo[3,4-h][1,4]benzoxazin-6-one
    参考文献:
    名称:
    Zur Umsetzung von 8a-Methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-onen mit Diazoalkanen, 2. Mitt.
    摘要:
    8a-Methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-ones 2 undergo regio- and stereospecific 1,3-dipolar cycloaddition reactions with diazomethane or diazoethane to yield 3,4,6 a,9,9 a,9 b-hexahydro-pyrazolo[3,4-h][1,4]benzoxazin-6(2H)-ones 3, which slowly isomerize in solution to give the 3,4,8,9,9a,9b-hexahydro-pyrazolo[3,4-h][1,4]benzoxazin-6(2H)-ones 5. The carbon of the diazoalkane dipole is attached to carbon C-8 of the benzoxazinone. The structures of the obtained products were determined by H-1- and C-13-NMR spectroscopy. An X-ray crystal structure analysis of 3a was carried out at room temperature: C11H15N3O3, M(r) = 237.26, orthorhombic, Pc2(1)n, a = 9.173 (5), b = 9.133 (4), c = 13.281 (6), V = 1112.6 (9) angstrom3, Z = 4, d(x) = 1.416 g/cm-3, mu = 0.93 cm-1, R = 4.33%, R(w) = 3.95% (919 observations, 168 parameters).
    DOI:
    10.1007/bf00811545
  • 作为产物:
    描述:
    8a-Hydroxy-4-<2-hydroxy-aethyl>-6-oxo-2,3,6,8a-tetrahydro-4H-1,4-benzoxazin碘甲烷silver(l) oxide 作用下, 以84%的产率得到4-(2-Hydroxyethyl)-8a-methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-on
    参考文献:
    名称:
    Zur Umsetzung von 8a-Methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-onen mit Diazoalkanen, 2. Mitt.
    摘要:
    8a-Methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-ones 2 undergo regio- and stereospecific 1,3-dipolar cycloaddition reactions with diazomethane or diazoethane to yield 3,4,6 a,9,9 a,9 b-hexahydro-pyrazolo[3,4-h][1,4]benzoxazin-6(2H)-ones 3, which slowly isomerize in solution to give the 3,4,8,9,9a,9b-hexahydro-pyrazolo[3,4-h][1,4]benzoxazin-6(2H)-ones 5. The carbon of the diazoalkane dipole is attached to carbon C-8 of the benzoxazinone. The structures of the obtained products were determined by H-1- and C-13-NMR spectroscopy. An X-ray crystal structure analysis of 3a was carried out at room temperature: C11H15N3O3, M(r) = 237.26, orthorhombic, Pc2(1)n, a = 9.173 (5), b = 9.133 (4), c = 13.281 (6), V = 1112.6 (9) angstrom3, Z = 4, d(x) = 1.416 g/cm-3, mu = 0.93 cm-1, R = 4.33%, R(w) = 3.95% (919 observations, 168 parameters).
    DOI:
    10.1007/bf00811545
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文献信息

  • 1,2-Oxazoline durch Addition von Trimethylbenzonitriloxid an 2-Hydroxyethylamino-1,4-benzochinone und deren Chinolderivate
    作者:Manfred Schubert-Zsilavecz、Dagmar Gusterhuber、Ferdinand Belaj
    DOI:10.1007/bf00810865
    日期:——
  • SCHUBERT-ZSILAVEEZ, MANFRED;GUSTERHUBER, DAGMAR;BELAJ, FERDINAND, MONATSH. CHEM., 121,(1990) N-7, C. 555-564
    作者:SCHUBERT-ZSILAVEEZ, MANFRED、GUSTERHUBER, DAGMAR、BELAJ, FERDINAND
    DOI:——
    日期:——
  • Zur Umsetzung von 8a-Methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-onen mit Diazoalkanen, 2. Mitt.
    作者:Manfred Schubert-Zsilavecz、Ferdinand Belaj、Robert Ott
    DOI:10.1007/bf00811545
    日期:1992.10
    8a-Methoxy-3,4-dihydro-2H-1,4-benzoxazin-6(8aH)-ones 2 undergo regio- and stereospecific 1,3-dipolar cycloaddition reactions with diazomethane or diazoethane to yield 3,4,6 a,9,9 a,9 b-hexahydro-pyrazolo[3,4-h][1,4]benzoxazin-6(2H)-ones 3, which slowly isomerize in solution to give the 3,4,8,9,9a,9b-hexahydro-pyrazolo[3,4-h][1,4]benzoxazin-6(2H)-ones 5. The carbon of the diazoalkane dipole is attached to carbon C-8 of the benzoxazinone. The structures of the obtained products were determined by H-1- and C-13-NMR spectroscopy. An X-ray crystal structure analysis of 3a was carried out at room temperature: C11H15N3O3, M(r) = 237.26, orthorhombic, Pc2(1)n, a = 9.173 (5), b = 9.133 (4), c = 13.281 (6), V = 1112.6 (9) angstrom3, Z = 4, d(x) = 1.416 g/cm-3, mu = 0.93 cm-1, R = 4.33%, R(w) = 3.95% (919 observations, 168 parameters).
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
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cnmr
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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